Yesterday Jen launched her exciting new mass-advocacy platform, #MEAction, and among its first actions is a mass petition to US Congress for equality for ME/CFS research funding - $250m a year.
Jen's prominence in the community gives this the potential to be hugely successful so let's get behind it!
It's automated and easy to do. I've already done it and sent a link to all my friends and family.
Here's the page for US people:
http://my.meaction.net/efforts/tell-congress-to-support-funding-equality-for-me-cfs/near/new
and here's the page for non-US people:
http://my.meaction.net/petitions/us...-around-the-world-care-about-funding-equality
Go, go, go!
Jen's prominence in the community gives this the potential to be hugely successful so let's get behind it!
It's automated and easy to do. I've already done it and sent a link to all my friends and family.
Here's the page for US people:
http://my.meaction.net/efforts/tell-congress-to-support-funding-equality-for-me-cfs/near/new
and here's the page for non-US people:
http://my.meaction.net/petitions/us...-around-the-world-care-about-funding-equality
Go, go, go!